Canonical Allele Identifier: CA327032000

Gene: PDHA1 MAP3K15

Linked Data

• dbSNP Id: rs898263736
• gnomAD v2: X-19378256-A-C
• gnomAD v3: X-19360138-A-C
• gnomAD v4: X-19360138-A-C
• MyVariant Identifiers: chrX:g.19378256A>C (hg19) ; chrX:g.19360138A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19360138A>C , CM000685.2:g.19360138A>C	GRCh38
NC_000023.10:g.19378256A>C , CM000685.1:g.19378256A>C	GRCh37
NC_000023.9:g.19288177A>C	NCBI36
NG_016781.1:g.21246A>C
NG_021184.1:g.160124T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*485A>C (PDHA1)	ENSP00000348062.6:n.*485A>C
ENST00000423505.6:c.*485A>C (PDHA1)	ENSP00000406473.2:n.*485A>C
ENST00000696704.1:c.*990A>C (PDHA1)	ENSP00000512823.1:n.*990A>C
ENST00000696705.1:c.*1113A>C (PDHA1)	ENSP00000512824.1:n.*1113A>C
ENST00000338883.9:c.*611T>G (MAP3K15) MANE Select	ENSP00000345629.4:n.*611T>G
ENST00000422285.7:c.*485A>C (PDHA1) MANE Select	ENSP00000394382.2:n.*485A>C
ENST00000359173.7:c.3881T>G (MAP3K15)
ENST00000379806.9:c.*485A>C (PDHA1)	ENSP00000369134.5:n.*485A>C
ENST00000422285.6:c.*485A>C (PDHA1)	ENSP00000394382.2:n.*485A>C
ENST00000470101.1:n.1971T>G (MAP3K15)
ENST00000518578.5:n.4615T>G (MAP3K15)
ENST00000540249.5:c.*485A>C (PDHA1)	ENSP00000440761.1:n.*485A>C
ENST00000545074.5:c.*485A>C (PDHA1)	ENSP00000438550.1:n.*485A>C
NM_000284.3:c.*485A>C (PDHA1)	NP_000275.1:n.*485A>C
NM_001001671.3:c.4553T>G (MAP3K15)	NP_001001671.3:n.4553T>G
NM_001173454.1:c.*485A>C (PDHA1)	NP_001166925.1:n.*485A>C
NM_001173455.1:c.*485A>C (PDHA1)	NP_001166926.1:n.*485A>C
NM_001173456.1:c.*485A>C (PDHA1)	NP_001166927.1:n.*485A>C
XM_011545507.1:c.*611T>G (MAP3K15)	XP_011543809.1:n.*611T>G
XM_011545508.1:c.*611T>G (MAP3K15)	XP_011543810.1:n.*611T>G
XM_011545509.1:c.*611T>G (MAP3K15)	XP_011543811.1:n.*611T>G
XM_011545510.1:c.*611T>G (MAP3K15)	XP_011543812.1:n.*611T>G
XM_011545511.1:c.*611T>G (MAP3K15)	XP_011543813.1:n.*611T>G
XM_011545531.1:c.*485A>C (PDHA1)	XP_011543833.1:n.*485A>C
XM_011545532.1:c.*485A>C (PDHA1)	XP_011543834.1:n.*485A>C
XM_011545507.3:c.*611T>G (MAP3K15)	XP_011543809.3:n.*611T>G
XM_011545508.3:c.*611T>G (MAP3K15)	XP_011543810.3:n.*611T>G
XM_011545510.2:c.*611T>G (MAP3K15)	XP_011543812.1:n.*611T>G
XM_011545511.2:c.*611T>G (MAP3K15)	XP_011543813.1:n.*611T>G
NM_000284.4:c.*485A>C (PDHA1) MANE Select	NP_000275.1:n.*485A>C
NM_001001671.4:c.*611T>G (MAP3K15) MANE Select	NP_001001671.3:n.*611T>G
NM_001173454.2:c.*485A>C (PDHA1)	NP_001166925.1:n.*485A>C
NM_001173455.2:c.*485A>C (PDHA1)	NP_001166926.1:n.*485A>C
NM_001173456.2:c.*485A>C (PDHA1)	NP_001166927.1:n.*485A>C